WordNet
- the means of connection between things linked in series (同)nexus
- a unit of length equal to 1/100 of a chain
- an interconnecting circuit between two or more locations for the purpose of transmitting and receiving data (同)data link
- a fastener that serves to join or connect; "the walls are held together with metal links placed in the wet mortar during construction" (同)linkup, tie, tie-in
- (computing) an instruction that connects one part of a program or an element on a list to another program or list
- the 24th letter of the Roman alphabet (同)x, ex
PrepTutorEJDIC
- (鎖の)『輪』,環 / 鎖のようにつながったソーセージの一節 / (…と)つなぐ物(人),(…との)きずな,つながり《+『with』(『to』)+『名』》 / 《複数形で》=cuff links / …‘を'『つなぎ合わせる』,連結する;(…と)…‘を'つなぐ《+『名』+『with』(『to』)+『名』》 / (…と)結合する,つながる《+[『up』(『together』)]『with』+『名』》
- たいまつ
- Christ / Christian
- x-axis
UpToDate Contents
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- 1. 色素沈着過剰を有する患者へのアプローチ approach to the patient with hyperpigmentation disorders
- 2. 小児および思春期における遺伝性再生不良性貧血 inherited aplastic anemia in children and adolescents
- 3. 先天性好中球減少症 congenital neutropenia
- 4. 健常者および患者における胎児性ヘモグロビン（ヘモグロビンF） fetal hemoglobin hemoglobin f in health and disease
- 5. 小児における血小板減少症の臨床症状および評価 clinical manifestations and evaluation of thrombocytopenia in children
English Journal
- A case of dyskeratosis congenita with dermoscopic and reflectance confocal microscopic features.
- Güngör Ş1, Erdemir AV2, Göncü EK3, Gürel MS2, Özekinci S4.
- Journal of the American Academy of Dermatology.J Am Acad Dermatol.2015 Jul;73(1):e11-3. doi: 10.1016/j.jaad.2015.02.1141.
- PMID 26089061
- Treatment of dyskeratosis congenita-associated pulmonary fibrosis with danazol.
- Zlateska B1,2, Ciccolini A1,2, Dror Y1,2.
- Pediatric pulmonology.Pediatr Pulmonol.2015 Jun 17. doi: 10.1002/ppul.23235. [Epub ahead of print]
- Individuals with Dyskeratosis Congenita (DC) are at increased risk for complications in variety of systems including pulmonary fibrosis. Idiopathic and DC-associated pulmonary fibrosis are progressive and fatal disorders without known treatment. Here we describe, for the first time, marked improveme
- PMID 26083318
- Triallelic and epigenetic-like inheritance in human disorders of telomerase.
- Collopy LC1, Walne AJ1, Cardoso S1, de la Fuente J2, Mohamed M3, Toriello H4, Tamary H5, Ling AJ1, Lloyd T1, Kassam R1, Tummala H1, Vulliamy TJ6, Dokal I1.
- Blood.Blood.2015 May 29. pii: blood-2015-03-633388. [Epub ahead of print]
- Dyskeratosis congenita (DC) and related diseases are a heterogeneous group of disorders characterized by impaired telomere maintenance, known collectively as the telomeropathies. Disease causing variants have been identified in ten telomere-related genes including the reverse transcriptase (TERT) an
- PMID 26024875
Japanese Journal
- Dyskeratosis congenita におけるDKC1遺伝子解析
- 金兼 弘和,野村 恵子,笠原 善仁,岡村 純,本郷 輝明,矢部 みはる,小島 勢二,鬼頭 敏幸,宮脇 利男
- 日本小児血液学会雑誌 16(2), 78-83, 2002-04-30
- NAID 10011415205
- Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in mice
- HE J
- Oncogene 21, 7740-7744, 2002
- NAID 30013802094
Related Links
- 305000 - DYSKERATOSIS CONGENITA, X-LINKED; DKCX - ZINSSER-COLE-ENGMAN SYNDROME - HOYERAAL-HREIDARSSON SYNDROME, INCLUDED; HHS, INCLUDED;; CEREBELLAR ... ...
- Dyskeratosis congenita is classically defined by the triad of abnormal skin pigmentation, nail dystrophy, and leukoplakia of the oral mucosa. It is characterized by short telomeres. Progressive bone marrow failure occurs in over 80% ...
Related Pictures
★リンクテーブル★
| リンク元 | 「X連鎖型先天性角化不全症」「X連鎖先天性角化不全症」 |
| 関連記事 | 「link」「congenita」「linked」「X」「dyskeratosis」 |
「X連鎖型先天性角化不全症」
「X連鎖先天性角化不全症」
「link」
- n.
- v.
- 関連づける、連結する、連接する
- 関
- associate、association、attach、bearing、bind、catenate、catenation、concatenation、connect、connection、correlate、correlation、implicate、implication、join、juncture、ligate、ligation、linkage、linked、pertinent、reference、relate、relation、relationship、relative、relevance、relevant
「congenita」
- adj.
- (後置するラテン語形容詞)先天性の
- ex.
「linked」
- adj.
- 連鎖の、連鎖的な、連鎖性の
「X」
「dyskeratosis」
- 異常角化、異常角化症